Minimal Residual Disease of T Acute Lymphoblastic Leukemia: the Experience of University Hospital Center Casablanca - Morocco [0.03%]
卡萨布兰加大学中心医院儿童T细胞急性淋巴细胞白血病微小残留病检测经验报告
Sara Addakiri,Hanaa Bencharef,Asmaa Harrach et al.
Sara Addakiri et al.
Background: MRD measurement is based on the ability to detect a minimal quantity of tumor cells within a population of healthy cells. Given the low sensitivity of cytology, flow cytometry in T-ALL allows the distinction b...
Jiehua Han,Qiongyin Xu
Jiehua Han
Background: Discrepancies between routine urinalysis and 24-hour urine protein quantification often indicate atypical pathologies. Light chain multiple myeloma (LCMM) secretes free light chains and may present conflicting...
Case Reports
Clinical laboratory. 2025 Oct 1;71(10). DOI:10.7754/Clin.Lab.2025.250343 2025
Interval Changes in Hematopoietic Vacuolization in VEXAS Syndrome with M41T Mutation: Insights into Diagnosis and Disease Progression [0.03%]
VEXAS综合征M41T突变患者的造血细胞空泡化间隔变化：诊断和疾病进展的新见解
Hyun-Woo Lee,SooHo Yu,Boram Kim et al.
Hyun-Woo Lee et al.
Background: VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is an adult-onset hemato-inflammatory disorder characterized by somatic mutations in the UBA1 gene on Xp11.3. We report a case of VEXAS...
Case Reports
Clinical laboratory. 2025 Oct 1;71(10). DOI:10.7754/Clin.Lab.2025.250314 2025
Combined Application of Multiple Technologies in Prenatal Diagnosis of a Fetus with Mosaic Isodicentric Y Chromosome [0.03%]
多项技术联合应用于嵌合型Y染色体等臂双着丝粒染色体胎儿的产前诊断
Tingting Luo,Ming Che,Lele Wang et al.
Tingting Luo et al.
Background: Isocentromere Y chromosome [idic(Y)] is a type of Y chromosome structural aberration, and patients have clinical manifestations such as Turner syndrome, unclear genitals, and male infertility. ...
Case Reports
Clinical laboratory. 2025 Oct 1;71(10). DOI:10.7754/Clin.Lab.2025.250333 2025
Difeng Chen,Minyan Zhao
Difeng Chen
Background: Platelets as one of the key indicators in blood tests, reflect the number of platelets in the blood, thereby aiding doctors in assessing the blood's coagulation and hemostatic functions. Abnormal platelet coun...
Case Reports
Clinical laboratory. 2025 Oct 1;71(10). DOI:10.7754/Clin.Lab.2025.250332 2025
The Effect of CALLY Index and HALP Score on Mortality in Patients with COVID-19 [0.03%]
CALLY指数和HALP评分对COVID-19患者死亡率的影响
Yeşim Yüksel,Özer E Gür,Rezarta T Senirli et al.
Yeşim Yüksel et al.
Background: The outbreak of the novel coronavirus disease (2019-nCoV) has become a significant public health concern, with the potential to cause a considerable number of deaths. The objective of this study was to examine...
Correlation between Lipoprotein(a) and Endometrial Cancer Prognosis: a Retrospective Cohort Study [0.03%]
脂蛋白(a)与子宫内膜癌预后的相关性研究：一项回顾性队列研究
Cong Liu,Zuommiao Xiao,Zhengting Liu et al.
Cong Liu et al.
Background: Endometrial cancer (EC) is a malignant tumor arising from the endometrial epithelium and is among the most prevalent gynecological malignancies worldwide. Increasing evidence suggests that lipid profiles, hype...
Serological Characteristics and Gene Sequencing of Rare A1.02/BA.04 Blood Type [0.03%]
罕见A1.02/BA.04血型的血清学特征和基因测序
Yongbo Liu,Jie Xue,Hongwei Qin
Yongbo Liu
Background: The typical serological profile of the B(A) subgroup is characterized by ABweak, with the primary genetic combination being heterozygosity between the B(A) allele and the O allele. When the B(A) allele is hete...
Case Reports
Clinical laboratory. 2025 Oct 1;71(10). DOI:10.7754/Clin.Lab.2025.250244 2025
Association between Anemia and Hyperuricemia: a Cross-Sectional Study [0.03%]
贫血与高尿酸血症的相关性分析：一项横断面研究
Zhengting Liu,Xianchun Chen
Zhengting Liu
Background: Recent epidemiological studies have suggested a potential correlation between anemia and hyperuricemia, yet the relationship within the American population remains unclear. This study intended to explore the p...
X-linked Adrenal Hypoplasia Congenita Patients Exhibiting Phenotypic Variability [0.03%]
临床表型多样的X-连锁先天性肾上腺发育不全患者
In Hwa Jeong,Sae Jin Kim,Jae Ho Yoo et al.
In Hwa Jeong et al.
Background: X-linked adrenal hypoplasia congenita (X-AHC) is a hereditary disease caused by pathogenic NR0B1 variants which result in primary adrenal insufficiency and hypogonadotropic hypogonadism. We report four male pa...
Case Reports
Clinical laboratory. 2025 Oct 1;71(10). DOI:10.7754/Clin.Lab.2025.250326 2025